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排序方式: 共有50条查询结果,搜索用时 703 毫秒
1.
用定量体积排除色谱方法研究了过渡金属Fe(Ⅲ)、Co(Ⅲ)、Cu(Ⅱ)、Ni(Ⅱ)的乙酰丙酮螯合物在四氢呋喃溶液中的加合和缔合行为。在溶液中乙酰丙酮钴(Ⅲ)以单个螯合物分子的形式存在,乙酰丙酮铜(Ⅱ)和乙酰丙酮铁(Ⅲ)与溶剂加合生成加合物,乙酰丙酮铁(Ⅲ)除加合物外还存在缔合度为2-10的多分散缔合物,乙酰丙酮镍(Ⅱ)水合物在四氢呋喃中产生了加合交换作用,同时存在缔合度为6左右的缔合物。色谱数据给出了螯合物、加合物及缔合物 相似文献
2.
On the self-association of the normal alcohols and the glass transition in alcohol-alcohol solutions
Arnold V. Lesikar 《Journal of solution chemistry》1977,6(2):81-93
The glass-transition temperature (Tg) in mutual binary mixtures of the primary alkanols from methanol throughn-octanol has been measured as a function of composition. For mixtures of the alkanols heavier than ethanol,T
g is found to be a linear function of the number-average molecular length. Methanol and ethanol mixtures show higherT
g values than indicated by this relation. These results are found to be consistent with association of the heavier alkanols into chains of very great length in the supercooled liquid, while ethanol and methanol must form networks with a moderate degree of crosslinking between chains. 相似文献
3.
We have analyzed decay kinetics of CF2 radicals in the afterglow of low-pressure, high-density C4F8 plasmas. The decay curve of CF2 density has been approximated by the combination of first- and second-order kinetics. The surface loss probability evaluated from the frequency of the first-order decay process has been on the order of 10–4. This small surface loss probability has enabled us to observe the second-order decay process. The mechanism of the second-order decay is self-association reaction between CF2 radicals (CF2+CF2C2F4). The rate coefficient for this reaction has been evaluated as (2.6–5.3)×10–14 cm3/s under gas pressures of 2 to 100 mTorr. The rate coefficient was found to be almost independent of the gas pressure and has been in close agreement with known values, which are determined in high gas pressures above 1 Torr. 相似文献
4.
We report the synthesis of three new dipyrrinone imine analogues and the characterisation of their self-association properties. Based on vapour pressure osmometry and nuclear magnetic resonance studies, placing the imine functional group at C(9) of the dipyrrinone disrupts the native self-association of the dipyrrinone core in a manner that correlates with the conformational A-value of the imine N-substituent. 相似文献
5.
The values of the gas-chromatographic indicator reflecting the capacity of analytes for self-association in pure liquids,
δT
b.p., were estimated for C1–C9 and C11
n-alkanols by capillary gas chromatography on a nonpolar stationary phase under isothermal conditions. The δT
b.p. values ofn-alkanols, found as the difference between the boiling points measured directly and those calculated from GC data, are correlated
with thermodynamic characteristics of the formation ofn-alkanol associates in pure liquids. Usingn-alkanols as analytes with insignificant temperature increments of the retention indices, it was shown that the δT
b.p. values can be determined under conditions used in gas chromatography with temperature programming. In this way a single chromatographic
run can be used to compare the capacities for self-association of analytes boiling over a wide temperature range. The C2–C9
n-alkanethiols, which are not associated in neat liquids, have negative δT
b.p. values. An interpretation of this finding is proposed.
Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 2, pp. 315–318 February, 2000. 相似文献
6.
S. F. Baranovskii P. A. Bolotin M. P. Evstigneev D. N. Chernyshev 《Journal of Applied Spectroscopy》2008,75(2):251-260
We have used spectrophotometry to study self-association and complexation with DNA by organic heterocyclic compounds in the
acridine and phenothiazine series: proflavin, thionine, and methylene blue. Based on the experimental concentration dependences
of the molar absorption coefficient of the molecules in an aqueous buffer solution (0.01 M NaCl, 0.01 M Na2EDTA, 0.01 M Tris, pH 7.4, T = 298 K), we have determined the equilibrium dimerization constants for the dyes and the DNA
complexation parameters using the Scatchard and McGhee-von Hippel models. The observed increase in the cooperativity parameters
as the dimerization constants of the ligands increase allowed us to hypothesize that the same interactions occur between dye
molecules adsorbed on DNA as in their self-association. The equilibrium DNA-binding constants for the ligands, obtained using
the McGhee-von Hippel cooperative model, are (20.9 ± 2.7)·103 M−1 for proflavin and (33.8 ± 4.1)·103 M−1 for thionine. Using the Scatchard model, taking into account intercalation and “external” binding of ligands with DNA, we
determined the DNA complexation constants for methylene blue: (26.4 ± 4.6)·103 and (96 ± 17)·103 M−1 respectively. Based on analysis of the data obtained, we hypothesized that the predominant type of binding with DNA is intercalation
binding in the case of proflavin and thionine, and “external” binding with the DNA surface in the case of methylene blue.
__________
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 75, No. 2, pp. 242–249, March–April, 2008. 相似文献
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10.
《Physics and Chemistry of Liquids》2012,50(2):67-75
Abstract Silver was electrodeposited on platinum electrodes from solutions of AgNO3 in NH3 at temperatures from ?70°C. to 140°C. The solutions were 0.036 molar in AgNO3 at ? 78°C. In the dense gaseous region, the concentrations of AgNO3 and NH3 were 0.018 and 22 moles/liter respectively. The deposit was observed to become more and more crystalline in appearance as the temperature approached the critical temperature of NH3(133°C). All electrodeposits at temperatures above 133°C were characterized by either dendritic or needle-like growths on sharp edges and corners. These were not observed at lower temperatures. Both three- and four-sided symmetries were observed, suggesting that the deposits were growing in the [111] and [100] directions, respectively. 相似文献